H-MAX System Surgical Technique

Transcription

H- MAX SYSTEM
Restoring
otion
SURGICAL TECHNIQUE
H-MAX SYSTEM SURGICAL TECHNIQUE
Index
Indications and contraindications
Pag.
>>
4
Stem sizes
Pag.
>>
7
Pre-operative planning
Pag.
>>
8
Stem size selection
Pag.
>>
9
Neck Resection
Pag.
>>
10
Femural preparation
Pag.
>>
11
Trial reduction
Pag.
>>
15
Definitive stem insertion H-MAX S
Pag.
>>
16
Definitive stem insertion H-MAX M
Pag.
>>
17
Definitive stem insertion H-MAX C
Pag.
>>
18
Definitive head insertion
Pag.
>>
19
Components removal
Pag.
>>
20
INSTRUMENT SET
Pag.
>>
22
PRODUCT CODES
Pag.
>>
26
SURGICAL TECHNIQUE
Limacorporate S.p.A. is a manufacturer of prosthetic implants and as such dœs not perform medical procedures.
This documentation concerning surgical techniques, which provides surgeons with general guidelines for implanting the
H-MAX stem, was developed with the advice of a team of surgical experts. All decisions as to the type of surgery and most
suitable technique are obviously the responsibility of the health care professional. Surgeons must make their own decisions as to
the adequacy of each planned implant technique based on their training, experience and the clinical condition of the patient.
For further information about our products, please visit our web site at www.limacorporate.com
LEONARDO DA VINCI: Vitruvian Man. Study of the proportions of the human body (circa 1490)
Indications, Contraindications and Warnings
INDICATIONS
CONTRAINDICATIONS
H-MAX stems are indicated for use in partial or total hip
Absolute contraindications include:
arthroplasty and they are intended for press-fit (uncement-
•
local or systemic infection;
ed) use. When used in total hip arthroplasty, monolithic ce-
•
septicaemia;
mentless stems are intended for use with modular heads
•
persistent acute or chronic osteomyelitis;
and compatible acetabular cups. When used in partial hip
•
confirmed nerve or muscle lesion compromising hip
arthroplasty, they are intended for use with femoral heads
joint function.
intended for partial hip arthroplasty or bipolar heads.
Hip arthroplasty is intended for reduction or relief of pain
Relative contraindications include:
and/or improved hip function in skeletally mature patients
•
vascular or nerve diseases affecting the concerned limb;
with the following conditions:
•
poor bone stock (for example due to osteoporosis or
extended previous revision surgery) compromising
•
osteoarthritis, avascular necrosis and dysplasia;
•
rheumatoid arthritis;
•
treatment of femoral head and neck fractures;
•
revisions in cases of good remaining femoral bone
stock.
•
metabolic disorders which may impair fixation and
stability of the implant;
•
any concomitant disease and dependence that might
affect the implanted prosthesis;
•
metal hypersensitivity to implant materials.
H-MAX M femoral stems are indicated also for correction
H-MAX M femoral stems are contraindicated also for pa-
of functional deformities.
tients with renal impairment (CoCrMo).
Please follow the instructions for use enclosed in
the product packaging.
4
the stability of the implant;
non-inflammatory degenerative joint disease including
Surgical Technique H-MAX SYSTEM
Indications, Contraindications and Warnings
RISK FACTORS
WARNINGS
The following risk factors may result in poor results with
The surgeon should carefully plan the surgery considering
this prosthesis:
the following:
•
overweight;
1.
•
strenuous physical activities (active sports, heavy
for patients with a small Intramedullary canal and/or
physical work);
metaphyseal region of the femur. The reduced size
•
fretting of modular junctions;
(M/L width) of these stems results in a corresponding
•
incorrect implant positioning (e.g varus positioning);
•
medical disabilities which can lead to an unnatural
Small sized stems: the Small sized stems are designed
reduction in the fatigue strength of the implant;
2.
High Offset combinations (use of lateralized stems): the
gait and loading of the hip joint;
lateralized stems are designed to restore the functional
•
muscle deficiencies;
offset of the hip joint to be comparable to that of the con-
•
multiple joint disabilities;
tralateral hip, however greater neck lengths are accompa-
•
refusal to modify postoperative physical activities;
nied by a higher risk of failure (e.g. breakage due to fatigue).
•
patient history of infections or falls;
Complications or failures of the total hip replacement are
•
systemic diseases and metabolic disorders;
more likely to occur in heavy and highly active patients and
•
local or disseminated neoplastic diseases;
high offset combinations. The surgeon should perform a
•
drug therapies that adversely affect bone quality,
careful evaluation of the patient’s clinical condition and lev-
healing, or resistance to infection
el of physical activity before performing hip replacement.
•
drug use or alcoholism;
Patients who are overweight (BMI >25 kg/m2) and/or
•
marked osteoporosis or osteomalacia;
have high activity levels and/or poor bone quality may
•
patient’s resistance to disease generally weakened
not be candidates for a modular hip replacement with
(HIV, tumour, infections);
H-MAX M femoral stems.
•
severe deformity leading to impaired anchorage or
improper positioning of implants
COMBINATIONS ALLOWED/NOT ALLOWED
Allowed combinations between Femoral head and H-MAX
M Modular necks:
•
With the exception of Lateralizing Long Modular necks
(#LAT-L), the modular necks can be coupled only with
S, M, L and XL femoral heads;
•
Lateralizing Long Modular necks (#LAT-L) can be
coupled only with S, M and L femoral heads. Use of
femoral heads with greater neck lengths may result in
failure of the hip stem (e.g. breakage due to fatigue).
The use of Ti6Al4V Modular necks is allowed only in
patients allergic to CoCrMo.
H-MAX SYSTEM Surgical Technique
5
Stem sizes
STEM SIZES
H-MAX S and H-MAX C are manufactured in 11 sizes for
the two versions standard and lateralizing. The H-MAX M
is available in 10 different sizes. The CCD in the standard
version is 134°; the CCD in the lateralizing version is 131°.
The dimension of the stems grows harmonically with size;
in the frontal view the increase in width is 1 mm for each
size. In the lateral view the thickness increases of 0.5 mm
for each size.
HORIZONTAL OFFSET TABLE FOR H-MAX S AND H-MAX C - monolithic stem with M size head
Size
STD
LAT
1
34.1 mm
39.1 mm
2
35.0 mm
40.0 mm
3
36.0 mm
41.0 mm
4
36.9 mm
41.9 mm
5
38.0 mm
43.0 mm
6
39.0 mm
44.0 mm
7
40.0 mm
45.0 mm
8
41.1 mm
46.0 mm
9
42.2 mm
47.2 mm
10
43.3 mm
48.3 mm
11
44.4 mm
49.4 mm
HORIZONTAL OFFSET TABLE FOR H-MAX M - modular stem with M size head
Size
STD SHORT NECK
STD-S (S1)
STD LONG NECK
STD-L (L1)
LAT SHORT NECK
LAT-S (S4)
LAT LONG NECK
LAT-L (L4)
1
34.7 mm
42.1 mm
39.7 mm
47.1 mm
2
35.1 mm
42.5 mm
40.1 mm
47.5 mm
3
35.6 mm
43,0 mm
40.6 mm
48.0 mm
4
36.1 mm
43.5 mm
41.1 mm
48.5 mm
5
36.5 mm
43.9 mm
41.5 mm
48.9 mm
6
37.1 mm
44.5 mm
42.1 mm
49.5 mm
7
37.6 mm
45.0 mm
42.6 mm
50.0 mm
8
38.4 mm
45.8 mm
43.4 mm
50.8 mm
9
38.8 mm
46.2 mm
43.8 mm
51.2 mm
10
39.5 mm
46.9 mm
44.5 mm
51.9 mm
7
Pre-operative Planning
PRE-OPERATIVE PLANNING
To obtain the best results, preoperative planning is recommended with the use of templates (showing a 15% enlarged image of the profiles).
Use good quality frontal and axial view radiographs with adequate contrast that are large enough to contain the entire
length of the pre-op template stems (Figs. 1-2).
Digital templates compatible with most surgical planning
software are also available.
Figure 1
RX with H-MAX S template
Figure 2
RX with H-MAX M template
8
Stem size selection
STEM SIZE SELECTION
To find the right stem size the contour lines of the proximal
part should fill the femoral epiphyseal region.
Make sure that the stem does not interfere with the femoral
curvature along the axial projection.
It is important to consider that the fixation of the stem is
obtained in the proximal part, therefore, the filling of the
canal is not required in the distal part.
Identify the size and type of neck to restore the correct
centre of rotation, checking the anteversion level in the
sagittal plane.
Identify the neck resection level by making the apex of the
Figure 3
H-MAX S Standard
Figure 4
H-MAX S Lateralizing
greater trochanter coincide with the centre of the medium
femoral head.
H-MAX S and C templates indicate the centre of rotation
in the two versions for the different lengths of the heads
(Figs. 3-4).
H-MAX M templates indicate the centre of rotation for the
different versions of the necks (standard short, standard-long, lateralizing short, lateralizing-long) and for the
different heads lenghts (Fig. 5).
H-MAX M templates also indicate the centre of rotation for
the versions standard-short and standard-long in the axial
projection (Fig. 6).
Note. Pre-operative planning provides useful indications
for the use of the the implant but does not definitely extabilish the size of the stem to be used, which must be verified
Figure 5
Figure 6
H-MAX M
H-MAX M
during the surgery.
9
Neck resection
NECK RESECTION
After having dislocated the femur, the femoral head is
resected (Fig. 7).
Figure 7
10
Femur preparation
FEMUR PREPARATION
Start preparing the canal with the box chisel, which allows
to open the greater trochanter area (Fig. 8).
Figure 8
The canal is then opened using a reamer (Fig. 9).
The H-MAX instrument set consists of a series of
broaches (Fig. 10); the broaches are connected to the
broach handles.
Figure 9
Figure 10
11
Femur preparation
Broach handles are available in the following versions:
“straight”, ‘’straight for Direct Anterior Approach “single
offset”, and “double offset” fitting to different surgical
approaches (Fig. 11a, b, c, d).
Figure 11a
Straight Handle
Figure 11b
Straight Handle for D.A.A.
Figure 11c
Curved Single-Offset Handle
Figure 11d
Double Offset Handle
12
Femur preparation
Connect the broach to the handle by lifting the lever and
inserting the broach with its medial part oriented towards
the lever (Fig. 12).
Tighten the lever until it is fully closed (Fig. 13).
Start broaching the canal using the smallest broach,
maintaining the correct anteversion (approx. 15°).
Insert the broach untill the tilted plane of the broach
coincides with the resection line of the neck.
Figure 12
Note. Trial reduction with broach #08 can be done for
H-MAX S and H-MAX C stems only (H-MAX M stem smallest size is #09).
Figure 13
13
Femur preparation
Note. The resection line is defined during the Pre operative
planning with the use of templates.
If the resection line results to be different from the planning
this difference has to be taken into account (Fig. 14 a, b, c).
Proceed with the next size up broach and continue until the
epiphyseal seat is filled properly.
Once the best broach size has been achieved (which may
not necessarily be the one planned during the preoperative
Figure 14a
planning), remove the handle and leave the broach in situ
(Fig. 14b).
Figure 14b
14
Figure 14c
Trial reduction
TRIAL REDUCTION
In case the acetabular component is implanted before the
femoral stem, a trial reduction can be performed.
The H-MAX M instrument set includes the trials of the 12
modular necks short (red) and long (grey) (Fig. 15).
Figure 15
The H-MAX S and C the instrument set includes the trials
for the necks in the two versions; standard (green) and lateralizing (blue) for each size (Fig. 16).
Insert the required trial neck with the neck positioner (Fig. 17).
Figure 16
Insert the trial head (Fig. 18) and perform the trial reduction
(Fig. 19).
Remove the trial neck using the neck extractor.
Figure 17
Figure 18
Figure 19
15
Definitive Stem Insertion H-MAX S
DEFINITIVE STEM INSERTION H-MAX S
The stem can be implanted using a screwed positioned
(A) or a free-hand impactor (B).
Figure 21
(A) Take the H-MAX S stem out of the box with the size
corresponding to the last broach used and remove it from
its sterile packaging. Screw the stem positioner on the deFigure 20
finitive stem (Fig. 20).
The washer indicates the locking/ unlocking direction
(Fig. 21). The T Wrench, inserted in the stem positioner,
it is useful to lock up the stem to the stem positioner (Fig.
22). After removing the T wrench it is possible to insert the
stem by impacting on the stem positioner.
The line of separation between the polished finishing and
the HA coating corresponds to the level reached by the
last broach used (Fig. 23).
(B) Manually insert the stem into the
femoral cavity,
align the free-hand impactor (available on request ref.
Figure 22
9095.11.111) on the lateral side of the stem (Fig. 24) and
impact until fully inserted.
Figure 24
Figure 23
16
Definitive Stem Insertion H-MAX M
DEFINITIVE STEM INSERTION H-MAX M
Take the H-MAX M stem out of the box with the size corresponding to the last broach used and remove it from its
sterile packaging (Fig. 25).
Figure 25
Using the broach handle, impact the stem, until the tilted plane of the stem reaches the level of the broach
(Figs. 26a, b, c).
The neck can be further checked by inserting the trial neck
on the final stem. Clean and dry the conical taper of the
stem. Take the definitive neck from the sterile packaging
and impact it with the neck positioner (Fig. 27) impacting
it on its axis.
Figure 26a
Figure 26b
Figure 27
Figure 26c
17
Definitive Stem Insertion H-MAX C
DEFINITIVE STEM INSERTION H-MAX C
After inserting the distal plug fill the femoral canal with acrylic cement from distal to proximal. Proceed with the introduction of the stem as for the H-MAX S as follows.
Please look at the LIMA-CMT 1, 2 and G brochure for in-
Figure 28
dication of the distal plug positioning and the cementing
procedure.
Figure 29
18
Definitive Head Insertion
DEFINITIVE HEAD INSERTION
Once the correct head size, diameter and material have
been chosein, the length of the head can be rechecked
using the trial heads. Take a head with the determined diFigure 30
ameter and length from its sterile packaging (Fig. 30).
Carefully clean and dry the neck taper, this is essential
when using ceramic heads, fix the head by pressing it in
and rotating it along the neck axis (Fig. 31).
Remove the protective cap and tap slightly along the cone
axis using the femoral head beater (available upon request)
(Fig. 32).
After having cleaned the articular surfaces, reduce the articulation (Fig. 33).
Figure 31
Note. For H-MAX M, with all “long” version necks, the use
of XL, XXL, XXXL head lenghts is not allowed.
Figure 32
Figure 33
19
Components removal
COMPONENTS REMOVAL
If necessary, the prosthetic components can be removed.
To remove the femoral head, simply tap the bottom of the
head in the axial direction using a beater.
Figure 34
Note. If only the head needs to be replaced, never use a
ceramic head on the same cone.
H-MAX S / H-MAX C
Screw the stem positioner on the stem. Screw the stem
extractor on the stem positioner and use the inertial
beater to extract the stem (Fig. 34).
H-MAX M
Remove the modular neck with the neck extractor (Fig. 35).
Lock the broach handle on the broach and beat backward
to extract the stem.
Figure 35
IMPORTANT: This method may be used in cases where
biological fixation is absent or weak; otherwise it may be
necessary to separate the integrated surfaces of the bone
using suitable scalpels.
20
Instrument Set
9042.05.000 H-MAX Common Instrument Set
22
Ref.
CODE
DESCRIPTION
Qty.
A
9042.05.080
Broach #08
1
A
9042.05.090
Broach #09
1
A
9042.05.100
Broach #10
1
A
9042.05.110
Broach #11
1
A
9042.05.120
Broach #12
1
A
9042.05.130
Broach #13
1
A
9042.05.140
Broach #14
1
A
9042.05.150
Broach #15
1
A
9042.05.160
Broach #16
1
A
9042.05.170
Broach #17
1
A
9042.05.180
Broach #18
1
B
9042.15.240
Neck Extractor
1
C
9042.20.110
Trial Neck STD - S
1
C
9042.20.130
Trial Neck STD - L
1
C
9042.20.210
Trial Neck STD - AVR / RVL - S
1
C
9042.20.230
Trial Neck STD - AVR / RVL - L
1
C
9042.20.310
Trial Neck STD - AVL / RVR - S
1
C
9042.20.330
Trial Neck STD - AVL / RVR - L
1
C
9042.25.110
Trial Neck LAT - S
1
C
9042.25.130
Trial Neck LAT - L
1
C
9042.25.210
Trial Neck LAT - AVR / RVL - S
1
C
9042.25.230
Trial Neck LAT - AVR / RVL - L
1
C
9042.25.310
Trial Neck LAT - AVL / RVR - S
1
C
9042.25.330
Trial Neck LAT - AVL / RVR - L
1
9042.05.950
Sterilizable Box
1
Instrument Set
9042.06.000 H-MAX Anterior/Lateral Approach Instrument Set
Ref.
CODE
DESCRIPTION
Qty.
A
9042.15.210
Reamer
1
B
9042.15.225
Broach Handle-Stem Positioner
2
C
9042.15.230
Neck Impactor
1
D
9095.10.160
Canal Chisel
1
E
9095.10.511
Trial Head Low Taper 12/14 Dia. 28mm S
1
E
9095.10.512
Trial Head Low Taper 12/14 Dia. 28mm M
1
E
9095.10.513
Trial Head Low Taper 12/14 Dia. 28mm L
1
9042.06.950
Sterilizable Box
1
DESCRIPTION
Qty.
9042.07.000 H-MAX Posterolateral/Lateral Approach Instrument Set
Ref.
CODE
A
9042.15.210
Reamer
1
B
9042.15.220
Straight Broach Handle-Stem
Positioner
2
C
9042.15.230
Neck Impactor
1
D
9095.10.160
Canal Chisel
1
E
9095.10.511
Trial Head Low Taper 12/14
Dia. 28mm S
1
E
9095.10.512
Dia. 28mm M
1
E
9095.10.513
Dia. 28mm
1
9042.07.950
Sterilizable Box
1
23
Instrument set
9042.08.000 Instrument Set for H-MAX S Femoral Stem
24
Ref.
CODE
DESCRIPTION
Qty.
A
A
9042.50.080
Trial Modular Neck #8
1
9042.50.090
1
A
9042.50.100
1
A
9042.50.110
1
A
9042.50.120
1
A
9042.50.130
1
A
9042.50.140
1
A
9042.50.150
1
A
9042.50.160
1
A
9042.50.170
1
A
9042.50.180
1
B
9042.51.080
Trial Lateralized Modular Neck #8
1
B
9042.51.090
1
B
9042.51.100
1
B
9042.51.110
1
B
9042.51.120
1
B
9042.51.130
1
B
9042.51.140
1
B
9042.51.150
1
B
9042.51.160
1
B
9042.51.170
1
B
9042.51.180
1
C
9046.10.230
Stem Positioner
1
D
9046.10.235
Stem Extractor
1
9042.08.920
Sterilizable box
1
Instrument set
9042.09.000 H-MAX Anterolateral Approach Instrument Set
Ref.
CODE
DESCRIPTION
Qty.
A
9042.15.210
Reamer
1
B
9042.15.215
Left Double Offset stem positioner
rasp-handpiece
1
B
9042.15.216
Right Double Offset stem positioner
rasp-handpiece
1
C
9042.15.230
neck Impactor
1
D
9095.10.160
diaphyseal canal chisel
1
E
9095.10.511
low taper trial head 12/14 Dia. 28mm S
1
E
9095.10.512 low taper trial head 12/14 Dia. 28mm M
1
E
9095.10.513
low taper trial head 12/14 Dia. 28mm L
1
9042.09.950
Sterilizable box
1
9095.11.112 Straight handle for D.A.A.
n
CODE
DESCRIPTION
9095.11.112
Straight handle for D.A.A
n upon request
9095.11.111 Free-hand impactor
n
CODE
DESCRIPTION
9095.11.111
Free-hand impactor
n upon request
25
Product codes
H-MAX S - STANDARD STEMS - TAPER 12/14
Ti6Al4V + HA
n 4250.20.080
#8
4250.20.090
#9
4250.20.100
# 10
4250.20.110
# 11
4250.20.120
# 12
4250.20.130
# 13
4250.20.140
# 14
4250.20.150
# 15
4250.20.160
# 16
4250.20.170
# 17
4250.20.180
# 18
n upon request
H-MAX S - LATERALIZING STEMS (OFFSET +5MM) - TAPER 12/14
Ti6Al4V + HA
n 4251.20.080
#8
4251.20.090
#9
4251.20.100
# 10
4251.20.110
# 11
4251.20.120
# 12
4251.20.130
# 13
4251.20.140
# 14
4251.20.150
# 15
4251.20.160
# 16
4251.20.170
# 17
4251.20.180
# 18
n upon request
26
Product codes
H-MAX M - MODULAR STEMS
Ti6Al4V + HA
4205.20.090
#9
4205.20.100
# 10
4205.20.110
# 11
4205.20.120
# 12
4205.20.130
# 13
4205.20.140
# 14
4205.20.150
# 15
4205.20.160
# 16
4205.20.170
# 17
4205.20.180
# 18
NECKS - TAPER 12/14
Modular necks
CoCrMo
4220.09.110
STD-S (S1)
4220.09.130
STD-L (L1)
4220.09.210
AVR/RVL-S (S2)
4220.09.230
AVR/RVL-L (L2)
4220.09.310
AVL/RVR-S (S3)
4220.09.330
AVL/RVR-L (L3)
Lateralizing modular necks
4225.09.110
LAT-S (S4)
4225.09.130
LAT-L (L4)
4225.09.210
LAT-AVR/RVL-S (S5)
4225.09.230
LAT-AVR/RVL-L (L5)
4225.09.310
LAT-AVL/RVR-S (S6)
4225.09.330
LAT-AVL/RVR-L (L6)
* IMPORTANT: . For allergic patients, modular necks in Titanium Ti6AI4V may be
used, code numbers 4220.12.xxx and, in the lateralizing version, code numbers
4225.15.xxx.
27
Product codes
H-MAX C - STANDARD STEMS - TAPER 12/14
FeCrNiMnMoNbN
4260.07.080
#8
4260.07.090
#9
4260.07.100
# 10
4260.07.110
# 11
4260.07.120
# 12
4260.07.130
# 13
4260.07.140
# 14
4260.07.150
# 15
4260.07.160
# 16
4260.07.170
# 17
4260.07.180
# 18
H-MAX C - LATERALIZING STEMS - TAPER 12/14
FeCrNiMnMoNbN
28
4261.07.080
#8
4261.07.090
#9
4261.07.100
# 10
4261.07.110
# 11
4261.07.120
# 12
4261.07.130
# 13
4261.07.140
# 14
4261.07.150
# 15
4261.07.160
# 16
4261.07.170
# 17
4261.07.180
# 18
Limacorporate spa
Via Nazionale, 52
33038 Villanova di San Daniele
Udine - Italy
Tel.: +39 0432 945511
Fax: +39 0432 945512
E-mail: [email protected]
www.limacorporate.com
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Tel.: +49 40 6378 4640
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Tel.: +34 93 228 9240
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Tel.: +421 484 161 133
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H-MAX System Surgical Technique

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